rs371077728

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs371077728(A;A)

Make rs371077728(A;G)

Reference

GRCh38 38.1/142

Chromosome

11

Position

94467821

Gene	MIR548L, MRE11A

is a	snp
is	mentioned by
dbSNP	rs371077728
dbSNP (classic)	rs371077728
ClinGen	rs371077728
ebi	rs371077728
HLI	rs371077728
Exac	rs371077728
Gnomad	rs371077728
Varsome	rs371077728
LitVar	rs371077728
Map	rs371077728
PheGenI	rs371077728
Biobank	rs371077728
1000 genomes	rs371077728
hgdp	rs371077728
ensembl	rs371077728
geneview	rs371077728
scholar	rs371077728
google	rs371077728
pharmgkb	rs371077728
gwascentral	rs371077728
openSNP	rs371077728
23andMe	rs371077728
SNPshot	rs371077728
SNPdbe	rs371077728
MSV3d	rs371077728
GWAS Ctlg	rs371077728

Max Magnitude

0

ClinVar
Risk	rs371077728(A;A) rs371077728(C;C) rs371077728(T;T)
Alt	rs371077728(A;A) rs371077728(C;C) rs371077728(T;T)
Reference	Rs371077728(G;G)
Significance	Other
Disease	Hereditary cancer-predisposing syndrome not specified
Variation	info
Gene	MIR548L MRE11A
CLNDBN	Hereditary cancer-predisposing syndrome not specified
Reversed	0
HGVS	NC_000011.9:g.94200987G>A; NC_000011.9:g.94200987G>C; NC_000011.9:g.94200987G>T
CLNSRC	Ambry Genetics ClinVar GeneDx
CLNACC	RCV000129234.5, RCV000115902.2, RCV000220133.1, RCV000166423.1,